Ab initio spectroscopy and thermochemistry of the platinum hydride ions, PtH+ and PtH

Rovibrational levels of low-lying electronic states of the gas-phase, diatomic molecules, PtH+ and PtH-, are computed on potential-energy functions obtained by using a hybrid spin-orbit configuration-interaction procedure. PtH- has a well-separated Σ0++1 ground state, while the first two electronic states of PtH+ (Σ0++1 and 3Δ3) are nearly degenerate. Combining the experimental photoelectron (PE) spectra of PtH- with theoretical photodetachment spectroscopy leads to an improved value for the electron affinity of PtH, EA(PtH) = (1.617 ± 0.015) eV. When PtH- is a product of photodissociation of PtHCO2-, its PE spectrum is broad because of rotational excitation. Temperature-dependent thermodynamic functions and thermochemistry of dissociation are computed from the theoretical energy levels. Previously published energetic quantities for PtH+ and PtH- are revised. The ground 1Σ+ term of PtH+ is not well described using single-reference theory.